# K252021: Disposable Endoscopic Injection Needles

- Pathway: 510(k) (Traditional)
- Applicant: Changzhou New Med Micro-Medtech Co., Ltd.
- Decided: Dec 2, 2025 after 155 days
- Product code: FBK (Endoscopic Injection Needle, Gastroenterology-Urology)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K955558 (1996). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K213914: Injection Needle, Jiangsu Vedkang Medical Science and Technology Co., Ltd. (2022) Summary page 5.

## Indications for use
This product is intended to be used in conjunction with an endoscope for the submucosal injection in the digestive tract.

Source page: https://510kreport.com/device/K252021
Methodology: https://510kreport.com/methodology